Cargando…
Two sides of the same coin: a complex presentation of autosomal dominant tubulointerstitial kidney diseases: a literature review and case reports
INTRODUCTION: Genetic kidney diseases are underdiagnosed; namely, from 7% to 40% of patients suffering from chronic kidney disease (CKD) can carry a pathogenic variant, depending on population characteristics. Hereditary tubulointerstitial kidney diseases, including autosomal dominant tubulointersti...
Autores principales: | Fistrek Prlic, Margareta, Huljev Frkovic, Sanda, Beck, Bodo, Tonkovic Durisevic, Ivana, Bulimbasic, Stela, Coric, Marijana, Lamot, Lovro, Ivandic, Ema, Vukovic Brinar, Ivana |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10667683/ https://www.ncbi.nlm.nih.gov/pubmed/38027261 http://dx.doi.org/10.3389/fped.2023.1283325 |
Ejemplares similares
-
Typical course of cystinuria leading to untypical complications in pregnancy: A case report and review of literature
por: Ivandic, Ema, et al.
Publicado: (2023) -
Predicting autosomal dominant polycystic kidney disease progression: review of promising Serum and urine biomarkers
por: Sorić Hosman, Iva, et al.
Publicado: (2023) -
Case report: Sevelamer-associated colitis—a cause of pseudotumor formation with colon perforation and life-threatening bleeding
por: Fistrek Prlic, Margareta, et al.
Publicado: (2023) -
Two novel variants in the lecithin:cholesterol acyltransferase gene resulted in classic LCAT deficiency
por: Fistrek Prlic, Margareta, et al.
Publicado: (2022) -
First Characterization of ADAMTS-4 in Kidney Tissue and Plasma of Patients with Chronic Kidney Disease—A Potential Novel Diagnostic Indicator
por: Vojtusek, Ivana Kovacevic, et al.
Publicado: (2022)